A short while ago we found out that our little Lena was born with cystic fibrosis; a disease that can seriously affect the lungs, pancreas, and other organs.
While CF care has come a long way, there is no known cure. Yet. That's why we've started a team in Lena's name for this fantastic fundraising event.
There are approximately 30,000 Americans living with cystic fibrosis. They are moms, dads, sisters, brothers, daughters, sons, and friends who struggle every day just to breathe. I walk for them. Will you join me and support my fundraising goal?
Salty kisses!
- Lena's Legion
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While CF care has come a long way, there is no known cure. Yet. That's why we've started a team in Lena's name for this fantastic fundraising event.
There are approximately 30,000 Americans living with cystic fibrosis. They are moms, dads, sisters, brothers, daughters, sons, and friends who struggle every day just to breathe. I walk for them. Will you join me and support my fundraising goal?
Salty kisses!
- Lena's Legion
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IMPORTANT NOTE ON ATTENDANCE AT FOUNDATION EVENTS:
Updated July 5th, 2023
The CF Foundation is committed to ensuring the health and wellbeing of individuals attending Foundation events. Individuals attending CF Foundation events must abide by the Foundation's Event Attendance Policy www.cff.org/attendancepolicy, which includes guidance for event attendees living with cystic fibrosis.